Medline recalls medical convenience kits due to removal difficulty and skin residue
Medline Industries is recalling 146,971 medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as Class II, involving medical convenience kits that are difficult to remove and leave adhesive residue on skin. The source does not report any illnesses, injuries, or deaths.
Plain-English summary
Medline Industries, LP is recalling 146,971 medical convenience kits. The recall was initiated due to reports that the products are difficult to remove from patients and leave adhesive residue on the patient's skin.
The affected products were distributed worldwide, including in the United States, Canada, Turkey, Australia, and the United Arab Emirates. The source text does not report any illnesses, injuries, or deaths associated with this recall.
Consumers and healthcare facilities should check their inventory for the specific Medline Kit Numbers, SKUs, and Lot Numbers listed in the official recall notice. If the products are found, they should be removed from use and returned to Medline Industries or the original supplier for credit or replacement.
The recalled product
- Product
- MEDLINE medical convenience kits labeled as: (list truncated)
- Manufacturer
- Medline Industries, LP
- Affected units
- 146,971
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Medline Kit Number/SKU DYNJ40917B
- UDI/DI 10195327599928 (each) 40195327599929 (case)
- Lot number 26HBB007
- Medline Kit Number/SKU DYNJ905792F
- UDI/DI 10198459411625 (each) 40198459411626 (case)
- Lot number 26FMH990
- Medline Kit Number/SKU CDSCCR611R
- UDI/DI 10198459001376 (each) 40198459001377 (case)
- Lot number 25KBM623
- Medline Kit Number/SKU CDSCCR611S
- UDI/DI 10198459610233 (each) 40198459610234 (case)
- Lot number 26HBE979
- Lot number 26GBK211
- Lot number 26EBK060
- Lot number 26ABQ736
- Lot number 26ABF499
- Medline Kit Number/SKU CDS820031J
- UDI/DI 10193489642971 (each) 40193489642972 (case)
- Lot number 26CMG521
- Lot number 25KBD161
Distribution
Distributed nationwide across the United States.
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